Deafness, Aminoglycoside-Induced (DFNI)

Alias:
Deafness, Mitochondrial, Modifier of
Aminoglycoside-Induced Deafness
Streptomycin Ototoxicity
Deafness, Streptomycin-Induced
Streptomycin-Induced Deafness
Dfni
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Deafness, Aminoglycoside-Induced, also known as deafness, mitochondrial, modifier of, is related to deafness, nonsyndromic sensorineural, mitochondrial and rare genetic deafness. An important gene associated with Deafness, Aminoglycoside-Induced is TRMU (TRNA Mitochondrial 2-Thiouridylase), and among its related pathways/superpathways is Complex I biogenesis. Affiliated tissues include bone, and related phenotypes are aminoglycoside-induced hearing loss and muscle
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Mit
Unknown
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15
127
13

Medical Symptom

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Description
HPO Frequency
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HPO Source Accession
No data available

Gene & Mutation

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Related Drugs

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No data available

Disease Model

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Name
MGI
Related Gene
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Publications
No data available

References Literature

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